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Merck
CN

387924

Poly(vinyl acetate)

average Mw ~140,000 by GPC

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About This Item

Linear Formula:
[CH2CH(O2CCH3)]n
CAS Number:
UNSPSC Code:
12162002
PubChem Substance ID:
MDL number:
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InChI

1S/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H3

SMILES string

COC(=O)C=C

InChI key

XTXRWKRVRITETP-UHFFFAOYSA-N

mol wt

average Mw ~140,000 by GPC

storage temp.

2-8°C

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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Congming Xiao et al.
International journal of biological macromolecules, 52, 349-352 (2012-10-31)
Tailor-made conjunct of methyl cellulose (MC) and polyvinyl acetate (PVAc) was synthesized through the combination of reversible addition-fragmentation chain transfer (RAFT) polymerization and thiol-ene click reaction. MC was firstly transferred into unsaturated MC (UMC), and then covalently connected with well-defined
V Andonova et al.
Die Pharmazie, 67(7), 601-604 (2012-08-15)
During the last decade the number of investigations on the preparation and application of more effective drug release systems on the basis of nanocarriers from biocompatible and biodegradable polymers are considerably increasing. This is notably in force for practically water
Il Gyu Kang et al.
American journal of rhinology & allergy, 24(5), 392-395 (2011-01-20)
The aim of this study was to evaluate the effect of repeated expandable polyvinyl acetate (EPA) packing for preventing stenosis of the frontal sinus ostium after patients undergo functional endoscopic sinus surgery (FESS). A nonrandomized, prospective study of 20 patients
Dong-Hao Zhang et al.
Bioresource technology, 124, 233-236 (2012-09-20)
Poly(vinyl acetate-acrylamide) microspheres were synthesized in the absence or presence of isooctane via suspension polymerization and utilized as carriers to immobilize Candida rugosa lipase. When the hydrophobic/hydrophilic surface characteristics of the microspheres were modified by changing the ratio of vinyl
Vibha Puri et al.
Journal of pharmaceutical sciences, 101(1), 342-353 (2011-09-22)
Amorphous solid dispersions (ASDs) may entail tailor-made dosage form design to exploit their solubility advantage. Surface phenomena dominated the performance of amorphous celecoxib solid dispersion (ACSD) comprising of amorphous celecoxib (A-CLB), polyvinylpyrrolidone, and meglumine (7:2:1, w/w). ACSD cohesive interfacial interactions

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